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Differential
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abdominal cramps
abducens nerve paralysis
acoustic nerve
adult polyglucosan body disease
ageusia
akathisia
alcohol intolerance
alkylating agents
altered states of consciousness
alternating hemiplegia
alternating hemiplegia of childhood
amyloidosis
anatomy of
angina pectoris
anhidrosis
anosmia
antimetabolite
areflexia
asparginase
asystole
ataxia
ataxia, cerebellar
ataxia, progressive
ataxic gait
atonic bladder
attention deficit disorder with hyperactivity
autonomic dysfunction
autonomic dysfunction, acute
autonomic nervous system
autonomic neuropathy
autonomic neuropathy, idiopathic
autosomal dominant leukodystrophy
axonal degeneration
Babinski sign
bacterial infection
baroreceptors
bladder dysfunction
blood dyscrasias, neurologic findings with
botulism
bradycardia
brain atrophy
brainstem, infarction of
bulbar palsy
burning paresthesia
carbamazepine
carcinoma
carcinoma of thyroid
CAT scan
CAT scan, abnormal
CAT scan, emission, abnormal
cataracts
cataracts, congenital
catecholamine
cerebellar atrophy, secondary
cerebellar vermis
cerebral cortical atrophy
cerebral ischemia
cerebral vasculature
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, pressure low
cerebrospinal fluid, xanthochromia of
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, young adult
cerebrovascular disease, cardiovascular disease with
Charcot-Marie-Tooth
chemotherapy, CNS treatment and complications with
chewing movements
children
chorea
choreoathetosis
cingulate island sign
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
coat-hanger pain
coma
confabulation
congestive heart failure
constipation
cranial neuropathy, multiple
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, familial
dementia, rapidly progressive
dementia, subcortical
developmental retardation
diabetes mellitus
diarrhea
differential diagnosis
diplopia
dopamine
drug induced neurologic disorders
dysarthria
dysdiadochokinesia
dysmetria
dysmorphic
dystonia
dystonia musculorum deformens
encephalopathy
erectile dysfunction
exome sequencing
eye, pain in
Fabry's disease
facial nerve palsy
facial nerve palsy, bilateral
facial pain
failure to thrive
falling
familial
familial rectal pain
fatal familial insomnia
fever
flunarizine
fluorouracil
flush syndrome
flushing
foot drop
Fragile-X associated tremor/ataxia-syndrome
fragile-X syndrome
gait disorder
gait, spastic
gamma amino butyric acid
gender
gene
gene mutation
genetic linkage
genetic neurologic disorders
genetic testing
Gilles de la Tourette syndrome
glycogen storage disease
hallucination
head injury
headache
hemiplegia
hepatic encephalopathy
hepatic encephalopathy, treatment of
homovanillic acid
Horner's syndrome
human immunodeficiency virus type 1
hydrocephalus
hyperhidrosis
hyperreflexia
hypertension
hyperthermia
hyponatremia
hyporeflexia
hyposmia
hypotension, neurologic causes of
hypotension, systemic
hypotonia
imbalance
immunotherapy
impotence
inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with
inattention
inclusion bodies
inclusion bodies, eosinophilic intranuclear
inclusion bodies, intranuclear
insight, loss
insomnia
intellectual deficit
intellectual deterioration
intrinsic hand muscles, wasting of
isoniazid
jaw pain
Jewish
karyotyping
Korsakoff's psychosis
laughing
laughing, pathologic
L-dopa
leprosy
leukemia, neurologic findings assoc.with
leukodystrophy
leukoencephalopathy
lipid storage disorder of CNS
marche a petits pas
masked facies
memory, defect of recent
memory, impairment of
meningismus
meningoencephalopathy
mental retardation
methotrexate
methylhydrazine derivatives
middle cerebellar peduncle, lesion, bilateral
misdiagnosis
monoamine oxidase inhibitors
monoamines
mortality
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, diffusion weighted
multiple endocrine neoplasia
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, misdiagnosis
multiple system atrophy
muscle pain
muscle weakness
myelomalacia
myeloneuropathy
myocardial infarction
myoclonic jerks
myoclonus
nausea and vomiting
neck pain
nerve biopsy
nerve growth factor
neuroendocrinology
neurofibromatosis 1
neurogenic bladder
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neuroma
neuronal intranuclear inclusion disease
neuropathology
neuropathology, brain
neuropathy
neuropathy, amyloid
neuropathy, diabetic
neuropathy, hereditary peripheral
neuropathy, peripheral
neuropathy, peripheral, treatment
neuropathy, sensory
neuropathy, sensory, hereditary
neuropathy, work up for
neurotoxin
neurotransmitter
next-generation sequencing
nitrogen mustard
norepinephrine
NOTCH2NLC
nystagmus
ocular dysmetria
orthostatic hypotension
orthostatic hypotension, idiopathic
pain
pain, anal
paraparesis
paratrigeminal syndrome
paresthesias
Parkinson disease
Parkinson disease, atypical
Parkinson disease, familial
Parkinsonism syndrome
paroxysmal extreme pain disorder
paroxysmal neurologic deficits
peroneal muscle atrophy, causes of
phenylketonuria
pleocytosis of cerebrospinal fluid
polyglucosan body
polyglucosan body disease
polyneuropathy, familial
precipitating factors
prion disease
procarbazine
prognosis
progressive neurologic disorder
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychosis
ptosis
ptosis, bilateral
pyramidal tract
pyramidal tract dysfunction
radiculopathy
review article
Riley-Day syndrome
Romberg's sign
screening
seizure
seizure, children
seizure, differential diagnosis of
sensorineural hearing loss
sensory ganglia
sensory ganglia, abnormal
shoulder, pain in
Shy-Drager syndrome
sick sinus syndrome
skin, biopsy
skin, lesions in neurologic disorders
sleep pathology and physiology
smell
SNCA duplication
sodium channel dysfunction
spasticity
spinal cord, lesion of
spinocerebellar ataxia
spinocerebellar ataxia type 3/Machado Joseph disease
stuporous
subcortical U fibers
syncope
tachycardia
tardive dyskinesia
taste
thalamus, atrophy of
thalamus, lesion of
thalamus, lesion of-bilateral
tinnitus
torticollis
transient neurologic deficit
trauma
treatment of neurologic disorder
tremor
tremor, intention
trichopoliodystrophy
trinucleotide repeats
urinary frequency
urinary incontinence
valsalva maneuver
vasospasm, cerebral
vinblastine
vincristine neurotoxicity
viral infection
visual loss, transient
vocal cord paralysis
weakness
weakness, progressive
weight loss
wheelchair
white matter disease
wide based gait
wrist drop
Showing articles 1500 to 1550 of 1945 << Previous Next >>

Familial Spastic Paraparesis & Deafness, A New X-Linked Neurodegenerative Disorder
Arch Neurol 43:943-946, Wells,C.R.&Jankovic,J., 1986

Preventive Screening for Fragile X Syndrome
Editorial, Lancet 2:1191-11921986., , 1986

Orthostatic Tremor in Familial-Essential Tremor
Neurol 36:1241-1245, Wee,A.S.,et al, 1986

Handedness & Essential Tremor
Arch Neurol 42:1082-1083, Biary,N.&Koller,W., 1985

Late-Onset Hallervorden-Spatz Disease Presenting as Familial Parkinsonism
Neurol 35:227-234, Jankovic,J.,et al, 1985

Neurological Findings in Patients with the Fragile-X Syndrome
JNNP 48:150-153, Finelli,P.F.,et al, 1985

Autonomic Neuropathy in Ocular Hypertension
Lancet 2:185-187, Clark,C.V.&Mapstone,R., 1985

Metachromatic Leukodystrophy Manifesting as a Schizophrenic Disorder:Computed Tomographic Correlation
Ann Neurol 18:94-95, Finelli,P.F., 1985

Peripheral Neuropathy in Cerebrotendinous Xanthomatosis
Arch Neurol 42:1008-1010, Katz,D.A.,et al, 1985

Olivopontocerebellar Atrophy with Dementia, Blindness, & Chorea, Response to Baclofen
Arch Neurol 42:757-758, Trauner,D.A., 1985

Dystonia & Calcification of the Basal Ganglia
Neurol 35:533-537, Larsen,T.A.,et al, 1985

Gilles de la Tourette's Syndrome, A Review of Clinical, Research & Future Directions for Investigation
Arch Neurol 42:393-397, Caine,E.D., 1985

Vacuolar Myelopathy Pathologically Resembling Subacute Combined Degeneration in Patients with AIDS
NEJM 312:874-879, Petito,C.K.,et al, 1985

MR Imaging in Fahr Disease
J Comput Assist Tomogr 9:790-792, Scotti,G.,et al, 1985

Adult GM1-Gangliosidosis:Clinical Patterns & Rectal Biopsy
Neurol 35:875-880, Nakano,T.,et al, 1985

Clinical Findings in Four Children with Biotinidase Deficiency Detected Through a Statewide Neonatal Screening Program
NEJM 313:16-19, 43-441985., Wolf,B.,et al, 1985

The Cherry-Red Spot in Tay-Sachs & Other Storage Diseases
Ann Neurol 17:356-360, Kivlin,J.D.,et al, 1985

Association Between Essential Tremor & Parkinson's Disease
Ann Neurol 17:329-333, Gereghty,J.J.,et al, 1985

Carbonic Anhydrase II Deficiency in 12 Families with Osteopetrosis with Renal Tubular Acidosis & Cerebral Calcification
NEJM 313:139-181, Sly,W.S.,et al, 1985

Neuroleptic Malignant Syndrome
NEJM 313:163-166, Guze,B.H.,et al, 1985

Febrile Convulsions in a National Cohort Followed up from Birth, I-Prevalence & Recurrence in the First Five Years of Life
BMJ 290:1307-1310, Verity,C.M.,et al, 1985

Portal-Systemic Myelopathy after Portacaval Shunt Surgery
Arch Int Med 145:1921-1922, Lebovics,E.,et al, 1985

Familial Syringomyelia
JNNP 48:936-938, Busis,N.A.&Hochberg,F.H., 1985

Diabetic Autonomic Neuropathy
Editorial, Lancet 1:379-3801985., , 1985

Autonomic Neuropathy Associated with Autoimmune Disease
Neurol 35:261-264, Gudesblatt,M.,et al, 1985

Cerebral Haemorrhagic Infarction in Young Patients with Hereditary Protein C Deficiency
BMJ 290:350-352, Wintzen,A.R.,et al, 1985

Atypical Alzheimer's Disease with Spastic Paresis & Ataxia
Ann Neurol 17:297-300, Aikawa,H.,et al, 1985

Autosomal Recessive Distal Muscular Dystrophy:A Comparative Study with Distal Myopathy with Rimmed Vacuole Formation
Ann Neurol 17:51-59, Nonaka,I.,et al, 1985

Familial Infantile Myasthenia Gravis
Arch Neurol 42:143-144, Gieron,M.A.,et al, 1985

Tangier Disease (Hypo-a-Lipoproteinemia)
Textbook of Child Neurology, 3rd Ed. , Phila, Lea & Febiger, Ch 1, p 86, Menkes,J.H., 1985

Long-Acting Propranolol in Essential Tremor
Neurol 35:108-110, Koller,W.C., 1985

Biotinidase Deficiency:Initial Clinical Features & Rapid Diagnosis
Ann Neurol 18:614-617, Wolf,B.,et al, 1985

Association of High Cyanide & Low Sulphur Intake in Cassava-Induced Spastic Paraparesis
Lancet 2:1211-1213, Cliff,J.,et al, 1985

Intracranial Calcification in Nephrogenic Diabetes Insipidus
JAMA 254:3349-3350, Kanzaki,S.,et al, 1985

GM1 Gangliosidosis:Clinical and Laboratory Findings in Eight Families
Hum Genet 70:347-354, Giugliani,R.,et al, 1985

Conjugal Multiple Sclerosis
In Handbook of Clinical Neurol, Elsivier Publ, Amsterdam 47:291985., Myrianthopoulos,N.C., 1985

Propranolol Therapy for Essential Tremor of the Head
Neurol 34:1077-1079, Koller,W.C., 1984

Clin. Path. Conference
Coproporphyria with Polyneuropathy, Case Record 39-1984, NEJM 311:839-847984., , 1984

Cancer in Relatives of Children with Central-Nervous-System Neoplasms
NEJM 311:749-753, Farwell,J.,et al, 1984

Recurrent Cranial Nerve Palsies
Clin Pearls 7:4-5, Aziz,N., 1984

Familial Occurrence of Amyotrophic Lateral Sclerosis, Parkinsonism, & Dementia
Ann Neurol 16:642-648, Schmitt,H.P.,et al, 1984

Diabetic Autonomic Neuropathy & Iritis:An Association Suggesting an Immunological Cause
BMJ 289:343-345, Guy,R.J.C.,et al, 1984

Myasthenia Gravis & Myasthenic Syndromes
Ann Neurol 16:519-534, Engel,A.G., 1984

MR Imaging of Familial Basilar Impression
J Comput Assist Tomogr 8:953-956, Bewermeyer,H.,et al, 1984

Central Nervous System Infections Associated with Hereditary Hemorrhagic Telangiectasia
Am J Med 77:86-92, Press,O.L.W.,et al, 1984

Iatrogenic Causalgia
Arch Neurol 41:821-824, Horowitz,S.H., 1984

Involvement of Upper-Airway Muscles in Extrapyramidal Disorders
NEJM 311:438-442, Vincken,W.G.,et al, 1984

Machado-Joseph-Azorean Disease
Arch Neurol 41:921-925, Fowler,H.L., 1984

Spasmodic Dysphonia
Lancet 2:1192, Gowers,W.R.,et al, 1984

Familial Multisystem Atrophy with Possible Thalamic Dementia
Neurol 34:1213-1217, Katz,D.A.,et al, 1984



Showing articles 1500 to 1550 of 1945 << Previous Next >>